CA1288884C - Elastomeres de silicone a un element, a faible consistance - Google Patents

Elastomeres de silicone a un element, a faible consistance

Info

Publication number: CA1288884C
Authority: CA; Canada
Prior art keywords: composition; silane; radicals; group; parts
Prior art date: 1985-09-27
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

CA000513192A

Other languages

English (en)

Inventor

Chi-Long Lee

Gary R. Homan

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Dow Silicones Corp

Original Assignee

Dow Corning Corp

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1985-09-27

Filing date

1986-07-07

Publication date

1991-09-10

1986-07-07 Application filed by Dow Corning Corp filed Critical Dow Corning Corp

1991-09-10 Application granted granted Critical

1991-09-10 Publication of CA1288884C publication Critical patent/CA1288884C/fr

2008-09-10 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

229920002379 silicone rubber Polymers 0.000 title claims abstract description 23
239000000203 mixture Substances 0.000 claims abstract description 141
229910000077 silane Inorganic materials 0.000 claims abstract description 52
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 51
239000000945 filler Substances 0.000 claims abstract description 31
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 19
238000002156 mixing Methods 0.000 claims abstract description 17
150000001451 organic peroxides Chemical class 0.000 claims abstract description 14
239000004945 silicone rubber Substances 0.000 claims abstract description 6
-1 polydimethylsiloxane Polymers 0.000 claims description 38
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 25
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
238000000034 method Methods 0.000 claims description 23
229920002554 vinyl polymer Polymers 0.000 claims description 15
239000004205 dimethyl polysiloxane Substances 0.000 claims description 13
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
BPMXEJSBTONLLG-UHFFFAOYSA-N n-[[acetyl(methyl)amino]-prop-1-enylsilyl]-n-methylacetamide Chemical group CC=C[SiH](N(C)C(C)=O)N(C)C(C)=O BPMXEJSBTONLLG-UHFFFAOYSA-N 0.000 claims description 12
TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 claims description 10
239000005909 Kieselgur Substances 0.000 claims description 9
229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 9
239000003094 microcapsule Substances 0.000 claims description 8
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 8
238000010438 heat treatment Methods 0.000 claims description 6
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 5
YLJJAVFOBDSYAN-UHFFFAOYSA-N dichloro-ethenyl-methylsilane Chemical compound C[Si](Cl)(Cl)C=C YLJJAVFOBDSYAN-UHFFFAOYSA-N 0.000 claims description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
239000010453 quartz Substances 0.000 claims description 4
229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
239000000463 material Substances 0.000 abstract description 14
230000009969 flowable effect Effects 0.000 abstract description 10
229920001296 polysiloxane Polymers 0.000 abstract description 7
238000004132 cross linking Methods 0.000 abstract description 6
230000000704 physical effect Effects 0.000 abstract description 6
238000004382 potting Methods 0.000 abstract description 5
229920000642 polymer Polymers 0.000 description 19
235000013870 dimethyl polysiloxane Nutrition 0.000 description 10
239000004615 ingredient Substances 0.000 description 10
150000003254 radicals Chemical class 0.000 description 10
238000003860 storage Methods 0.000 description 10
229920001971 elastomer Polymers 0.000 description 9
239000000806 elastomer Substances 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000011248 coating agent Substances 0.000 description 6
238000000576 coating method Methods 0.000 description 6
239000012298 atmosphere Substances 0.000 description 5
238000001723 curing Methods 0.000 description 5
150000002978 peroxides Chemical class 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
239000000377 silicon dioxide Substances 0.000 description 5
WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 0.000 description 4
239000004970 Chain extender Substances 0.000 description 4
239000011347 resin Substances 0.000 description 4
229920005989 resin Polymers 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
239000004005 microsphere Substances 0.000 description 3
239000012763 reinforcing filler Substances 0.000 description 3
235000012239 silicon dioxide Nutrition 0.000 description 3
GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 3
238000012360 testing method Methods 0.000 description 3
DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
238000005266 casting Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
230000001419 dependent effect Effects 0.000 description 2
239000012153 distilled water Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
238000005538 encapsulation Methods 0.000 description 2
239000003517 fume Substances 0.000 description 2
FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
239000012778 molding material Substances 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
150000004756 silanes Chemical class 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical group C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 description 2
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
JBKVHLHDHHXQEQ-UHFFFAOYSA-N Caprolactam Natural products O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
239000005046 Chlorosilane Substances 0.000 description 1
FDEJNNNVDVOMKI-UHFFFAOYSA-N N-[(N-acetylanilino)-prop-1-enylsilyl]-N-phenylacetamide Chemical compound CC=C[SiH](N(C(C)=O)C1=CC=CC=C1)N(C(C)=O)C1=CC=CC=C1 FDEJNNNVDVOMKI-UHFFFAOYSA-N 0.000 description 1
IMPVGWPSUORTEQ-UHFFFAOYSA-N N-[[acetyl(ethyl)amino]-prop-1-enylsilyl]-N-ethylacetamide Chemical compound CC=C[SiH](N(C(C)=O)CC)N(C(C)=O)CC IMPVGWPSUORTEQ-UHFFFAOYSA-N 0.000 description 1
OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
230000004913 activation Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
235000006708 antioxidants Nutrition 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000001175 calcium sulphate Substances 0.000 description 1
235000011132 calcium sulphate Nutrition 0.000 description 1
238000003490 calendering Methods 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
239000012969 di-tertiary-butyl peroxide Substances 0.000 description 1
238000009792 diffusion process Methods 0.000 description 1
238000003618 dip coating Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000013536 elastomeric material Substances 0.000 description 1
238000010292 electrical insulation Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
239000012535 impurity Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
238000011068 loading method Methods 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
239000012766 organic filler Substances 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000007493 shaping process Methods 0.000 description 1
FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
229920002050 silicone resin Polymers 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
239000010887 waste solvent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/10—Encapsulated ingredients
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/14—Peroxides
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/541—Silicon-containing compounds containing oxygen
- C08K5/5425—Silicon-containing compounds containing oxygen containing at least one C=C bond
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/544—Silicon-containing compounds containing nitrogen
- C08K5/5455—Silicon-containing compounds containing nitrogen containing at least one group
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/544—Silicon-containing compounds containing nitrogen
- C08K5/5477—Silicon-containing compounds containing nitrogen containing nitrogen in a heterocyclic ring
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/549—Silicon-containing compounds containing silicon in a ring

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Silicon Polymers (AREA)

CA000513192A 1985-09-27 1986-07-07 Elastomeres de silicone a un element, a faible consistance Expired - Lifetime CA1288884C (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US780,747		1985-09-27
US06/780,747 US4614760A (en)	1985-09-27	1985-09-27	Low consistency, one-part silicone elastomers

Publications (1)

Publication Number	Publication Date
CA1288884C true CA1288884C (fr)	1991-09-10

Family

ID=25120558

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000513192A Expired - Lifetime CA1288884C (fr)	1985-09-27	1986-07-07	Elastomeres de silicone a un element, a faible consistance

Country Status (4)

Country	Link
US (1)	US4614760A (fr)
EP (1)	EP0216390A3 (fr)
JP (1)	JPS62109852A (fr)
CA (1)	CA1288884C (fr)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2621923A1 (fr) *	1987-10-20	1989-04-21	Rhone Poulenc Chimie	Composition organopolysiloxane a fonction cetiminoxy comportant un hydrogel comme agent de durcissement
US4882369A (en) *	1988-04-15	1989-11-21	Dow Corning Corporation	High strength fluorosilicone sealants
US5171773A (en) *	1991-11-13	1992-12-15	Dow Corning Corporation	High strength fluorosilicone rubber
JPH06329997A (ja) *	1993-05-18	1994-11-29	Toray Dow Corning Silicone Co Ltd	シリコーンゴムによる基材の接着方法
JPH06329914A (ja) *	1993-05-18	1994-11-29	Toray Dow Corning Silicone Co Ltd	室温硬化性オルガノポリシロキサン組成物およびその製造方法
US5854310A (en) *	1997-07-21	1998-12-29	Dow Corning Corporation	Curable fluorosilicone composition having improved lubricity
US8346337B2 (en)	1998-04-30	2013-01-01	Abbott Diabetes Care Inc.	Analyte monitoring device and methods of use
US8480580B2 (en)	1998-04-30	2013-07-09	Abbott Diabetes Care Inc.	Analyte monitoring device and methods of use
US8974386B2 (en)	1998-04-30	2015-03-10	Abbott Diabetes Care Inc.	Analyte monitoring device and methods of use
US8465425B2 (en)	1998-04-30	2013-06-18	Abbott Diabetes Care Inc.	Analyte monitoring device and methods of use
US6949816B2 (en)	2003-04-21	2005-09-27	Motorola, Inc.	Semiconductor component having first surface area for electrically coupling to a semiconductor chip and second surface area for electrically coupling to a substrate, and method of manufacturing same
US6175752B1 (en)	1998-04-30	2001-01-16	Therasense, Inc.	Analyte monitoring device and methods of use
US9066695B2 (en)	1998-04-30	2015-06-30	Abbott Diabetes Care Inc.	Analyte monitoring device and methods of use
US8688188B2 (en)	1998-04-30	2014-04-01	Abbott Diabetes Care Inc.	Analyte monitoring device and methods of use
JP4671461B2 (ja) *	2000-01-24	2011-04-20	コニシ株式会社	長期粘度安定性、作業適性及びヘラ切れ性に優れたシーリング材組成物
US6560471B1 (en)	2001-01-02	2003-05-06	Therasense, Inc.	Analyte monitoring device and methods of use
WO2002078512A2 (fr)	2001-04-02	2002-10-10	Therasense, Inc.	Dispositif et procede de recherche de glucose dans le sang
KR20040031021A (ko) *	2001-08-29	2004-04-09	다우 코닝 도레이 실리콘 캄파니 리미티드	저비중 액체 실리콘 고무 조성물 및 이로부터 성형된 제품
US20050003216A1 (en) *	2003-06-30	2005-01-06	Jean-Marc Frances	Microparticle containing silicone release coatings having improved anti-block and release properties
DE102005008951A1 (de) *	2005-02-24	2006-09-07	Wacker Chemie Ag	Siliconkautschukmassen und daraus erhaltene dauerbelastungsbeständige Siliconelastomere
ES2387896T3 (es)	2005-04-06	2012-10-03	Dow Corning Corporation	Composiciones de organosiloxano
BRPI0711694B8 (pt)	2006-04-20	2021-07-27	Aortech Biomaterials Pty Ltd	géis bioestáveis, biomaterial, dispositivo, artigo ou implante, e material de carga para um implante médico
US20080071157A1 (en)	2006-06-07	2008-03-20	Abbott Diabetes Care, Inc.	Analyte monitoring system and method
GB0905205D0 (en)	2009-03-26	2009-05-13	Dow Corning	Preparation of organosiloxane polymer
GB0905204D0 (en)	2009-03-26	2009-05-13	Dow Corning	Preparation of organosiloxane polymers

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE795952A (fr) *	1972-09-29	1973-08-27	Dow Corning	Compositions d'elastomere de silicone a faible module durcissables a la temperature ambiante
US3766128A (en) *	1972-09-29	1973-10-16	Dow Corning	Silicone elastomer composition containing amidosilane and aminosilane
US3766127A (en) *	1972-09-29	1973-10-16	Dow Corning	Amidosilicon low modulus room temperature vulcanizable silicone elastomer
US4020044A (en) *	1975-07-16	1977-04-26	Dow Corning Corporation	Method of increasing the molecular weight of hydroxyl endblocked polydiorganosiloxanes
US4347336A (en) *	1981-10-13	1982-08-31	Dow Corning Corporation	Heat cured silicone elastomer

1985
- 1985-09-27 US US06/780,747 patent/US4614760A/en not_active Expired - Fee Related
1986
- 1986-07-07 CA CA000513192A patent/CA1288884C/fr not_active Expired - Lifetime
- 1986-09-26 JP JP61226380A patent/JPS62109852A/ja active Pending
- 1986-09-26 EP EP86113268A patent/EP0216390A3/fr not_active Withdrawn

Also Published As

Publication number	Publication date
EP0216390A3 (fr)	1988-05-25
US4614760A (en)	1986-09-30
EP0216390A2 (fr)	1987-04-01
JPS62109852A (ja)	1987-05-21

Legal Events

Date	Code	Title	Description
1995-03-11	MKLA	Lapsed

Publication	Publication Date	Title
CA1288884C (fr)	1991-09-10	Elastomeres de silicone a un element, a faible consistance
US4162243A (en)	1979-07-24	High strength, extrudable silicone elastomer compositions
US4500659A (en)	1985-02-19	Extrudable, curable polyorganosiloxane compositions
US4448927A (en)	1984-05-15	Method of polymerizing oligomers of polydiorganosiloxane in the presence of filler
US4387177A (en)	1983-06-07	Room temperature curable organopolysiloxane compositions and methods for their preparation
US4360610A (en)	1982-11-23	Method of improving silicone rubber composition
CN101772551B (zh)	2013-05-29	基于有机硅化合物的可交联物质
US4490500A (en)	1984-12-25	Completely solventless two component RTV silicone composition
US2927907A (en)	1960-03-08	Siloxane elastomers
US4066603A (en)	1978-01-03	Sulfur containing silicone elastomer and method of preparation
US2902467A (en)	1959-09-01	Siloxane-silicate elastomers
EP0489391A2 (fr)	1992-06-10	Compositions organosiloxane durcissables aptes à l'extrusion
US4124560A (en)	1978-11-07	Two-component silicone rubber
US4174338A (en)	1979-11-13	Pasty compositions for crosslinking organopolysiloxanes to silicone rubber
US5206329A (en)	1993-04-27	One part heat curable organopolysiloxane compositions
US5246980A (en)	1993-09-21	Two-part, ultralow modulus silicone sealant
US3280072A (en)	1966-10-18	Organopolysiloxane elastomers
JPS6147172B2 (fr)	1986-10-17
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